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Focuses on understanding the relationship between an organism's genome and its phenotype, particularly the functions of genes and non-coding regions of the genome.

Used to identify similarities and differences between DNA, RNA, or protein sequences, which can infer functional, structural, or evolutionary relationships.

The study of the complete set of epigenetic modifications on the genetic material of a cell, which can affect gene expression without altering the DNA sequence.

Allows researchers to compare a query sequence with a library or database of sequences, and identify library sequences that resemble the query sequence above a certain threshold.

The process of putting together sequences from short DNA fragments, which reveals the complete genome sequence of an organism.

Applied to analyze complex patterns in genomic data, which can lead to the discovery of new genetic features and understandings of disease mechanisms.

Combines chromatin immunoprecipitation with sequencing to identify the binding sites of DNA-associated proteins.

Used to detect the expression of thousands of genes simultaneously or to genotype multiple regions of a genome.

Essential for studying genetic variation between individuals and populations, which can be associated with disease and response to drugs.

Predicts the three-dimensional structure of a protein from its amino acid sequence, which can provide insights into the protein's function.

Enables the study of an organism's transcriptome, the complete set of RNA transcripts produced by the genome at any one time.

A genetic engineering tool used to edit genomes with high precision, which has revolutionized genetics by enabling targeted modifications to DNA.

The study of the evolutionary history and relationships among individuals or groups of organisms.

The study of genetic material recovered directly from environmental samples, which can be used to understand microbial communities and diversity.